Canonical Allele Identifier: CA3261180214
Community Standard Title: NM_058216.3(RAD51C):c.1063_1065delinsCGG (p.Cys355Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734154_58734156delinsCGG , CM000679.2:g.58734154_58734156delinsCGG GRCh38
NC_000017.10:g.56811515_56811517delinsCGG , CM000679.1:g.56811515_56811517delinsCGG GRCh37
NC_000017.9:g.54166514_54166516delinsCGG NCBI36
NG_023199.1:g.46553_46555delinsCGG , LRG_314:g.46553_46555delinsCGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1063_1065delinsCGG MANE Select NP_478123.1:p.Cys355Arg
ENST00000337432.9:c.1063_1065delinsCGG MANE Select ENSP00000336701.4:p.Cys355Arg
NM_058216.2:c.1063_1065delinsCGG NP_478123.1:p.Cys355Arg
NR_103872.1:n.967_969delinsCGG
NR_103872.2:n.938_940delinsCGG
ENST00000337432.8:c.1063_1065delinsCGG ENSP00000336701.4:p.Cys355Arg
ENST00000413590.5:c.704_706delinsCGG
ENST00000461271.6:c.*1595_*1597delinsCGG ENSP00000464056.2:n.*1595_*1597delinsCGG
ENST00000461706.1:n.250_252delinsCGG
ENST00000475762.5:c.*1699_*1701delinsCGG ENSP00000432421.1:n.*1699_*1701delinsCGG
ENST00000482007.5:c.*491_*493delinsCGG ENSP00000433332.1:n.*491_*493delinsCGG
ENST00000487525.5:c.*639_*641delinsCGG ENSP00000431637.1:n.*639_*641delinsCGG
ENST00000578151.1:n.276_278delinsCGG
ENST00000581221.5:n.578_580delinsCGG
ENST00000584804.1:c.297_299delinsCGG ENSP00000463658.1:p.Val100Gly
ENST00000697680.1:c.*2027_*2029delinsCGG ENSP00000513392.1:n.*2027_*2029delinsCGG
ENST00000697681.1:c.*2224_*2226delinsCGG ENSP00000513393.1:n.*2224_*2226delinsCGG
ENST00000697683.1:c.*1999_*2001delinsCGG ENSP00000513395.1:n.*1999_*2001delinsCGG
ENST00000697685.1:c.*1760_*1762delinsCGG ENSP00000513396.1:n.*1760_*1762delinsCGG
ENST00000697686.1:c.834_836delinsCGG ENSP00000513397.1:p.Val279Gly
ENST00000697689.1:c.*1477_*1479delinsCGG ENSP00000513398.1:n.*1477_*1479delinsCGG
ENST00000697690.1:c.*23_*25delinsCGG ENSP00000513399.1:n.*23_*25delinsCGG
ENST00000697691.1:c.*1035_*1037delinsCGG ENSP00000513400.1:n.*1035_*1037delinsCGG
ENST00000697692.1:c.*1075_*1077delinsCGG ENSP00000513401.1:n.*1075_*1077delinsCGG
ENST00000697694.1:c.712_714delinsCGG ENSP00000513402.1:p.Cys238Arg
ENST00000697695.1:n.1670_1672delinsCGG
XM_006722001.2:c.1066_1068delinsCGG XP_006722064.1:p.Cys356Arg
XM_006722001.4:c.1066_1068delinsCGG XP_006722064.1:p.Cys356Arg
XM_006722002.2:c.1002_1004delinsCGG XP_006722065.1:p.Val335Gly
XM_006722002.4:c.1002_1004delinsCGG XP_006722065.1:p.Val335Gly
XM_006722004.2:c.715_717delinsCGG XP_006722067.1:p.Cys239Arg
XM_006722004.3:c.715_717delinsCGG XP_006722067.1:p.Cys239Arg
XM_006722005.2:c.715_717delinsCGG XP_006722068.1:p.Cys239Arg
XM_006722005.3:c.715_717delinsCGG XP_006722068.1:p.Cys239Arg
XM_011525092.1:c.715_717delinsCGG XP_011523394.1:p.Cys239Arg
XM_011525092.2:c.715_717delinsCGG XP_011523394.1:p.Cys239Arg
XM_011525093.1:c.715_717delinsCGG XP_011523395.1:p.Cys239Arg
XM_011525093.2:c.715_717delinsCGG XP_011523395.1:p.Cys239Arg
XM_011525094.1:c.715_717delinsCGG XP_011523396.1:p.Cys239Arg
XM_011525094.2:c.715_717delinsCGG XP_011523396.1:p.Cys239Arg
XM_017024914.1:c.712_714delinsCGG XP_016880403.1:p.Cys238Arg
XM_017024915.1:c.712_714delinsCGG XP_016880404.1:p.Cys238Arg
XM_017024916.1:c.712_714delinsCGG XP_016880405.1:p.Cys238Arg
XM_017024917.1:c.712_714delinsCGG XP_016880406.1:p.Cys238Arg
XM_017024918.2:c.712_714delinsCGG XP_016880407.1:p.Cys238Arg
XM_017024919.1:c.651_653delinsCGG XP_016880408.1:p.Val218Gly
XR_934513.1:n.1281_1283delinsCGG
XR_934513.3:n.1712_1714delinsCGG
XR_934514.1:n.1284_1286delinsCGG
XR_934514.3:n.1715_1717delinsCGG
XR_934886.1:n.149+3915_149+3917delinsCCG
XR_934886.2:n.149+3915_149+3917delinsCCG